确定假尿嘧啶掺入对人trna的影响。

Anna D Biela,Jakub S Nowak,Artur P Biela,Sunandan Mukherjee,Seyed Naeim Moafinejad,Satyabrata Maiti,Andrzej Chramiec-Głąbik,Rahul Mehta,Jakub Jeżowski,Dominika Dobosz,Priyanka Dahate,Veronique Arluison,Frank Wien,Paulina Indyka,Michal Rawski,Janusz M Bujnicki,Ting-Yu Lin,Sebastian Glatt
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引用次数: 0

摘要

转移RNA (trna)是一种普遍存在的非编码RNA分子,用于将mrna编码的序列信息翻译成新生的多肽链。它们相对较小的尺寸和其RNA修饰的异质性模式阻碍了单个trna的系统结构表征。在这里,我们使用单粒子冷冻电镜(cryo-EM)来确定掺入假尿嘧啶前后的四种人类trna的结构(Ψ)。经过不同组合的人假尿嘧啶合成酶的转录后修饰,我们发现trna变得稳定,并经历特定的局部结构变化。我们建立了D臂和t臂之间的相互作用作为trna三级结构的关键关键。我们的人类trna结构突出了冷冻电镜结合生物物理测量和计算模拟的巨大潜力,用于trna和其他小的折叠RNA结构域的结构-功能分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determining the effects of pseudouridine incorporation on human tRNAs.
Transfer RNAs (tRNAs) are ubiquitous non-coding RNA molecules required to translate mRNA-encoded sequence information into nascent polypeptide chains. Their relatively small size and heterogenous patterns of their RNA modifications have impeded the systematic structural characterization of individual tRNAs. Here, we use single-particle cryo-EM to determine the structures of four human tRNAs before and after incorporation of pseudouridines (Ψ). Following post-transcriptional modifications by distinct combinations of human pseudouridine synthases, we find that tRNAs become stabilized and undergo specific local structural changes. We establish interactions between the D- and T-arms as the key linchpin in the tertiary structure of tRNAs. Our structures of human tRNAs highlight the vast potential of cryo-EM combined with biophysical measurements and computational simulations for structure-function analyses of tRNAs and other small, folded RNA domains.
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